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Abstract #25785 Published in IGR 12-2

Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: Structure-based drug design, synthesis, and biological evaluation

Vernier W; Chong W; Rewolinski D; Greasley S; Pauly T; Shaw M; Dinh D; Ferre RA; Nukui S; Ornelas M
Bio-organic and Medicinal Chemistry 2010; 18: 3307-3319


A novel series of potent thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV was discovered using structure-based drug design. Synthesis, structure-activity relationship, and optimization of physicochemical properties are described. Low nanomolar potency was achieved, and selected compounds with improved thermodynamic solubility showed promising in vitro inhibition of carbonic anhydrase activity in rabbit iris ciliary body homogenate.

W. Vernier. Pfizer Global Research and Development, La Jolla Laboratories, 10770 Science Center Drive, San Diego, CA 92121, United States. william.f.vernier@pfizer.com


Classification:

11.14 Investigational drugs; pharmacological experiments (Part of: 11 Medical treatment)



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